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Long Noncoding RNAs with snoRNA Ends

文献类型:期刊论文

作者Yin, QF; Yang, L; Zhang, Y; Xiang, JF; Wu, YW; Carmichael, GG; Chen, LL
刊名MOLECULAR CELL
出版日期2012
卷号48期号:2页码:219-230
通讯作者Carmichael, GG (reprint author), Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Stem Cell Inst, Farmington, CT 06030 USA.,carmichael@nso2.uchc.edu ; linglingchen@sibcb.ac.cn
英文摘要We describe the discovery of sno-IncRNAs, a class of nuclear-enriched intron-derived long noncoding RNAs (IncRNAs) that are processed on both ends by the snoRNA machinery. During exonucleolytic trimming, the sequences between the snoRNAs are not degraded, leading to the accumulation of IncRNAs flanked by snoRNA sequences but lacking 5' caps and 3' poly(A) tails. Such RNAs are widely expressed in cells and tissues and can be produced by either box C/D or box H/ACA snoRNAs. Importantly, the genomic region encoding one abundant class of sno-IncRNAs (15q11-q13) is specifically deleted in Prader-Willi Syndrome (PWS). The PWS region sno-IncRNAs do not colocalize with nucleoli or Cajal bodies, but rather accumulate near their sites of synthesis. These sno-IncRNAs associate strongly with Fox family splicing regulators and alter patterns of splicing. These results thus implicate a previously unannotated class of IncRNAs in the molecular pathogenesis of PWS.
学科主题Biochemistry & Molecular Biology; Cell Biology
类目[WOS]Biochemistry & Molecular Biology ; Cell Biology
关键词[WOS]SMALL NUCLEOLAR RNA ; PRADER-WILLI-SYNDROME ; MAMMALIAN-CELLS ; STEM-CELLS ; PROTEIN ; NUCLEAR ; INTRON ; FOX-1 ; IDENTIFICATION ; TRANSCRIPTION
收录类别SCI
语种英语
WOS记录号WOS:000310423800008
版本出版稿
源URL[http://202.127.25.143/handle/331003/539]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
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GB/T 7714
Yin, QF,Yang, L,Zhang, Y,et al. Long Noncoding RNAs with snoRNA Ends[J]. MOLECULAR CELL,2012,48(2):219-230.
APA Yin, QF.,Yang, L.,Zhang, Y.,Xiang, JF.,Wu, YW.,...&Chen, LL.(2012).Long Noncoding RNAs with snoRNA Ends.MOLECULAR CELL,48(2),219-230.
MLA Yin, QF,et al."Long Noncoding RNAs with snoRNA Ends".MOLECULAR CELL 48.2(2012):219-230.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

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